SARS-CoV-2 Nucleoprotein Recombinant Protein (N-His-SUMO & C-Avi) (VK805062)

Name: SARS-CoV-2 Nucleoprotein Recombinant Protein (N-His-SUMO & C-Avi)
Brand: abinScience
SKU: VK805062
Price: 211 USD
Availability: InStock

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Overview

Catalog No.	VK805062
Description	Recombinant SARS-CoV-2 Nucleoprotein, N-His-SUMO & C-Avi (VK805062) expressed in E. coli. Purity: >90% as determined by SDS-PAGE.. Highlights ●E. coli Expression — High-yield, cost-effective production. ●High Purity — >90% as determined by SDS-PAGE.
Expression system	E. coli
Accession	P0DTC9
Protein length	Asn47-Ala173
Applications	ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Species	Severe acute respiratory syndrome coronavirus 2
Nature	Recombinant
Endotoxin level	Please contact with the lab for this information.
Purity	>90% as determined by SDS-PAGE.
Form	Lyophilized
Storage buffer	Lyophilized from a solution in PBS pH 7.4, 1 mM EDTA, 4% Trehalose, 1% Mannitol. Please refer to the specific buffer information in the hardcopy of datasheet or the lot-specific COA.
Reconstitution	Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.
Shipping	In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.
Stability and Storage	Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Alternate Names	N, NC, Nucleocapsid protein, Nucleoprotein, Protein N
Background	Nucleoprotein is a ~45 kDa protein. Packages the positive strand viral genome RNA into a helical ribonucleocapsid (RNP) and plays a fundamental role during virion assembly through its interactions with the viral genome and membrane protein M. Plays an important role in enhancing the efficiency of subgenomic viral RNA transcription as well as viral replication. Attenuates the stress granules formation by reducing host G3BP1 access to host mRNAs under stress conditions. 1. Dinesh, DC. et al. (2020) PLoS pathogens 16, e1009100. PMID: 33264373 2. Nabeel-Shah, S. et al. (2022) iScience 25, 103562. PMID: 34901782 3. Dolliver, SM. et al. (2022) PLoS pathogens 18, e1011041. PMID: 36534661
Note	For research use only